提供FDA注册，食品FDA注册、化妆品FDA注册，美国代理人服务、FDA验厂、FDA警告性移除
美国代理人职责 美国代理人作为FDA和国外工厂之间的交流纽带，负责紧急情况和日常事务交流。当发生紧急情况时，FDA会联系美国代理人，除非注册时指定另一个作为紧急情况联系人。美国代理人代表国外工厂，FDA将视美国代理人的陈述为国外工厂的陈述，并且将会认为向美国代理人提供的信息或文件等同于向国外工厂提供了信息或文件。 美国代理人注意事项 美国代理人不能只是邮箱、语音电话，或者作为国外工厂代理人的个人地址根本就不存在的场所。美国代理必须能随时接听FDA打来的电话。FDA会不定期随机地与美国代理人联系，对于信息不真实的代理人，FDA会要求工厂提供真实信息，否则，会进行处罚，甚至注销工厂的注册编号。 二、器械申请FDA注册（企业注册和产品列名） FDA企业注册定义 依据21 CFR Part 807的要求，FDA要求所有生产和销售到美国本土的器械厂商都应进行工厂注册。对于美国本土以外的企业，需要指定美国代理人并在企业注册时候得到美国代理人的确认方能生效。
Responsibilities of a U.S. agent The U.S. agent must either reside in the U.S. or maintain a place of business in the U.S. The U.S. agent cannot use a post office box as an address. The U.S. agent cannot use an answering service. They must be available to answer the phone or have an employee available to answer the phone during normal business hours. The responsibilities of the U.S. agent are limited and include: assisting FDA in communications with the foreign establishment, responding to questions concerning the foreign establishment's devices that are imported or offered for import into the United States, assisting FDA in scheduling inspections of the foreign establishment and if FDA is unable to contact the foreign establishment directly or expeditiously, FDA may provide information or documents to the U.S. agent, and such an action shall be considered to be equivalent to providing the same information or documents to the foreign establishment. Please note that the U.S. agent has no responsibility related to reporting of adverse events under the Medical Device Reporting regulation (21 CFR Part 803), or submitting 510(k) Premarket Notifications (21 CFR Part 807, Subpart E).
检查结果： 1.没有书面评价，这是好的情况； 2.轻微项的483表，或一封感谢信； 3.有批评的483表，它可能会导致：1）Seizure（查封）2）Detention(扣押)3）Restraining Orders and Injunctions(强制停产)4）Penalties（罚款）5）Recall（撤回） 4. Waring letter（警告信）审核重点：对于不同的产品，审核的重点不一样的